Liu M - Search Results

1

Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population.

Ren X, Xu C, Zhan C, Yang Y, Shi L, Wang F, Wang C, Xia Y, Yang B, Wu G, Wang P, Li X, Wang D, Xiong X, Liu J, Liu Y, Liu M, Liu J, Tu X, Wang QK. Ren X, et al. Among authors: liu j, liu y, liu m. Clin Chim Acta. 2010 Apr 2;411(7-8):481-5. doi: 10.1016/j.cca.2009.12.019. Epub 2010 Jan 11. Clin Chim Acta. 2010. PMID: 20064500

2

Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome.

Fan C, Liu M, Wang Q. Fan C, et al. Among authors: liu m. J Biol Chem. 2003 Mar 7;278(10):8780-5. doi: 10.1074/jbc.M208120200. Epub 2002 Dec 23. J Biol Chem. 2003. PMID: 12499378 Free PMC article.

3

Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a Chinese family.

Wang Q, Liu M, Xu C, Tang Z, Liao Y, Du R, Li W, Wu X, Wang X, Liu P, Zhang X, Zhu J, Ren X, Ke T, Wang Q, Yang J. Wang Q, et al. Among authors: liu m, liu p. J Mol Med (Berl). 2005 Mar;83(3):203-8. doi: 10.1007/s00109-005-0638-4. Epub 2005 Feb 22. J Mol Med (Berl). 2005. PMID: 15726306 Free PMC article.

4

[Advances in the studies on the molecular and genetic aspects of epilepsy].

Wang X, Wang T, Yuan MX, Liu MG, Wang Q. Wang X, et al. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005 Jun;27(3):388-93. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2005. PMID: 16038283 Review. Chinese.

5

Genetic analysis of a family with 46,XY "female" associated with infertility.

Wang X, Wang XR, Liu MG, Wang Q, Liu JY. Wang X, et al. Yi Chuan Xue Bao. 2006 Jan;33(1):19-25. doi: 10.1016/S0379-4172(06)60003-6. Yi Chuan Xue Bao. 2006. PMID: 16450583

6

Two novel missense mutations of GATA4 gene in Chinese patients with sporadic congenital heart defects.

Tang ZH, Xia L, Chang W, Li H, Shen F, Liu JY, Wang Q, Liu MG. Tang ZH, et al. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006 Apr;23(2):134-7. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2006. PMID: 16604480

7

[Mutation of Thr704Met in SCN 4A causes normoKPP in a Chinese family].

Ren X, Bu BT, Yao Q, Qiu X, Liu JY, Wang Q, Liu MG. Ren X, et al. Yi Chuan. 2006 Aug;28(8):923-6. Yi Chuan. 2006. PMID: 16870577 Chinese.

8

A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.

Liu M, Wang X, Cai Z, Tang Z, Cao K, Liang B, Ren X, Liu JY, Wang QK. Liu M, et al. Among authors: liu jy. J Hum Genet. 2006;51(8):727-731. doi: 10.1007/s10038-006-0012-6. Epub 2006 Jul 27. J Hum Genet. 2006. PMID: 16871364

9

Novel HSF4 mutation causes congenital total white cataract in a Chinese family.

Ke T, Wang QK, Ji B, Wang X, Liu P, Zhang X, Tang Z, Ren X, Liu M. Ke T, et al. Among authors: liu m, liu p. Am J Ophthalmol. 2006 Aug;142(2):298-303. doi: 10.1016/j.ajo.2006.03.056. Am J Ophthalmol. 2006. PMID: 16876512

10

Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.

Liu M, Ke T, Wang Z, Yang Q, Chang W, Jiang F, Tang Z, Li H, Ren X, Wang X, Wang T, Li Q, Yang J, Liu J, Wang QK. Liu M, et al. Among authors: liu j. Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3461-6. doi: 10.1167/iovs.05-1438. Invest Ophthalmol Vis Sci. 2006. PMID: 16877416

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